Cargando…
A rare case of Swyer syndrome from Pakistan in a young girl with primary amenorrhea and 46XY genotype
Swyer syndrome is a condition where individuals with a 46XY karyotype, typically associated with males, display complete gonadal dysgenesis and lack testicular differentiation. This results from a mutation in the SRY gene, which is essential for testis development. As a consequence, affected individ...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666715/ https://www.ncbi.nlm.nih.gov/pubmed/37994022 http://dx.doi.org/10.1177/17455057231213270 |